Zobrazeno 1 - 10
of 217
pro vyhledávání: '"Zinner syndrome"'
Publikováno v:
BMC Urology, Vol 24, Iss 1, Pp 1-5 (2024)
Abstract Background Zinner syndrome (ZS) is a congenital malformation characterized by a triad of mesonephric (Wolffian) duct dysplasia, first identified by Zinner in 1914. The classical presentation of ZS includes unilateral renal hypoplasia or dysp
Externí odkaz:
https://doaj.org/article/9541411a355442bfadd552b1f253779b
Autor:
Meriem Boui, Meryem Edderai, Ouijdane Zamani, Ouadie El Menaoui, Abdelaziz Hommadi, Mohamed Lahkim, Hassan Boumdine, Tarik Salaheddine, Hassan En-Nouali, Jamal El Fenni, Rachida Saouab
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 5586-5588 (2024)
Zinner syndrome is a rare congenital malformation characterized by cystic seminal vesicles and ejaculatory duct obstruction in association with ipsilateral renal agenesis. It appears to be frequently linked to infertility. However, recent advances in
Externí odkaz:
https://doaj.org/article/60026785c2d446398ebd21801fcc95b1
Publikováno v:
IJU Case Reports, Vol 7, Iss 5, Pp 383-386 (2024)
Introduction This report describes a case with an ectopic ejaculatory duct opening into the bladder trigone in Zinner syndrome, congenital unilateral renal agenesis, and an ipsilateral seminal vesicle cyst. Case presentation The patient was identifie
Externí odkaz:
https://doaj.org/article/4110b43e6aed42a09e6d9483b62b07b2
Publikováno v:
Radiology Case Reports, Vol 19, Iss 7, Pp 2663-2668 (2024)
Zinner syndrome comprises a triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction, which can be accompanied by additional abnormalities of the genitourinary tract in some cases. Patients may be asympto
Externí odkaz:
https://doaj.org/article/50fe244a4ab34c58830a3e6d2c1689c0
Publikováno v:
Asian Journal of Surgery, Vol 47, Iss 8, Pp 3714-3716 (2024)
Externí odkaz:
https://doaj.org/article/ff8c0e349bee43b5b3f11928bdbaa40a
Publikováno v:
Xin yixue, Vol 55, Iss 5, Pp 342-347 (2024)
Objective To investigate the key issues of clinical diagnosis and treatment of Zinner syndrome and reduce the misdiagnosis rate. Methods Clinical data of 1 case of Zinner syndrome were retrospectively analyzed. Zinner syndrome cases presenting hematu
Externí odkaz:
https://doaj.org/article/681cde71be7c4d2e8d11c1bd76797754
Publikováno v:
Urology Case Reports, Vol 56, Iss , Pp 102818- (2024)
Zinner Syndrome (ZS) is a rare congenital genitourinary abnormality defined by seminal vesicle cysts, ejaculatory duct obstruction, and unilateral renal dysplasia or agenesis. Patients can be asymptomatic, while others experience pain, urinary or eja
Externí odkaz:
https://doaj.org/article/cc34d50d04534f41893d89496b113031
Autor:
João Ferreira Guerra, João Magalhães Pina, Vanessa Andrade, Miguel Brito Lança, Luís Campos Pinheiro
Publikováno v:
Український Журнал Нефрології та Діалізу, Iss 3(83) (2024)
Zinner Syndrome (ZS) is a rare congenital malformation characterized by a triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction. Typically discovered incidentally in the second to fourth decades of lif
Externí odkaz:
https://doaj.org/article/ec02cd94ea6c4feb9949bc28929c8118
Autor:
Ottavio Adorisio, Cinzia Orazi, Lorenzo Maria Gregori, Francesco De Peppo, Massimiliano Silveri
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
IntroductionZinner syndrome (ZS) is the association of seminal vesicle cysts, ipsilateral ejaculatory duct obstruction, and ipsilateral renal agenesis. This condition is very rare in children and both diagnosis and treatment may be challenging. We re
Externí odkaz:
https://doaj.org/article/f76b5446dc924ce8870e0bfb90d9e91b
Autor:
Ali Zare, MD, Behzad Narouie, MD, Farzad Moloudi, MD, Fatemeh Moosavian, MD, Mohadese Ahmadzade, MD, Hamidreza Rouientan, MD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 11, Pp 4103-4105 (2023)
Zinner Syndrome is a rare congenital anomaly. It is considered a rare cause of male infertility and can cause a range of clinical manifestations that may lead to significant morbidity. The diagnosis of Zinner Syndrome requires a high index of suspici
Externí odkaz:
https://doaj.org/article/0ded5a47f26c4d098f9ec57b79b42534